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NCT04888078 Clinical Trial

Bassini Inguinal Hernia Repair: Obsolete Or Still A Viable Surgical Option?

Inguinal Hernia Clinical Trial

Official title:
Incidence of POUR in the Veteran Population After Elective Inguinal Hernia Repair: A Retrospective Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04888078
Other study ID # 02331
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2006
Est. completion date December 31, 2019

Study information
Verified date May 2021
Source Hunter Holmes Mcguire Veteran Affairs Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Retrospective review of hernia surgery patients at HHMcGuire VAMC focusing on repair type and postoperative complications.

Recruitment information / eligibility
Status Completed
Enrollment 203
Est. completion date December 31, 2019
Est. primary completion date December 31, 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: Inguinal hernia repair without mesh - Exclusion Criteria: Mesh repair -

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Bassini hernia repair
Non-mesh tissue inguinal hernia repairs

Locations
Country Name City State
United States Hunter Holmes McGuire VAMC Richmond Virginia

Sponsors (1)
Lead Sponsor Collaborator
Hunter Holmes Mcguire Veteran Affairs Medical Center

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Inguinal hernia recurrence chart review 5-13 years postoperatively
Secondary wound infection chart review 5-13 years
Secondary urinary retention chart review 5-13 years
Secondary groin pain chart review 5-13 years
Secondary durability of repair chart review 5-13 years postop
Secondary testicular ischemia chart review 5-13 years
See also
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Completed NCT02240550 - A Comparative Clinical Study to Evaluate the Effectiveness of ProFlor vs. Lichtenstein for Inguinal Hernia Repair N/A
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Completed NCT01117337 - Comparing Non-fixation of Mesh to Mesh Fixation in Laparoscopic Inguinal Hernia Repair Phase 4
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Recruiting NCT05879770 - Is the Use of Prolene as Sufficient as the Use of Wire in Shouldice Surgery to Keep the Recurrence Rate Low After One Year?
Completed NCT05159232 - Length of Hospital Stay in Laparoscopic Transabdominal Preperitoneal Vs. Open Mesh Repair in Inguinal Hernia: A Randomised Controlled Trial N/A
Completed NCT05107986 - Laparoscopy in Complicated Groin Hernia
Active, not recruiting NCT04328597 - Portuguese Inguinal Hernia Cohort (PINE) Study
Completed NCT04033055 - Antalgic Efficacy of CycloMesh™ Soaked in Ropivacaine Hydrochloride in Uncomplicated Inguinal Hernia. N/A